Tag | Content |
---|
EnhancerAtlas ID | HS182-09259 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:27216390-27217500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr17:27216969-27216982 | AATTAATTAATTC | - | 6.29 | Lhx3 | MA0135.1 | chr17:27216968-27216981 | TAATTAATTAATT | + | 6.78 | NKX2-3 | MA0672.1 | chr17:27216443-27216453 | TTCAAGTGGT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr17:27216876-27216891 | CGAACTCTTGACCTT | - | 6.06 | POU6F1 | MA0628.1 | chr17:27216970-27216980 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr17:27216970-27216980 | ATTAATTAAT | - | 6.02 | Sox3 | MA0514.1 | chr17:27217217-27217227 | AAAACAAAGG | - | 6.02 |
|
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_53891 | chr17:27216825-27217527 | Spleen | SE_59217 | chr17:27214241-27230502 | Ly3 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I028890 | chr17 | 27216826 | 27217527 |
|
Enhancer Sequence | AGGCTAGACT ACAGTGGCGC AGTCTCGGCT CACTGCAACC TCTGCCTCCT GGGTTCAAGT 60 GGTTCTCCTG CCTCAGCCTC CTGAGTTGCT GGGATCACAG GTGCCCGCCA CAGCATACCT 120 GGCTAATTTT TGTATTTTTA GTACAGACAG AGTTTCATCA TGTTGGCCAG GCTGGTCTCA 180 AACTCTTGGC CTTAGGCAAT CTGCCTGCCT TGGCCTCCCA AAGTGCTGGC ATTACAGGTG 240 TGAGCCACCT CGCCAGGCCA GCTTCCTTTT TTTTTGGTTT TTCTGGAGAT GGAGTTTTGC 300 TCTGTTGCCC AGGCTGGAGT GCAGTGGCGT GATCTTGGCT CACTGCAACC TCTGCCTCCC 360 AGGTTCAAGC AATTCTCCTG CCTCAGCCTC CCGAGTAGCT GGGATTACAG GCATGCATCA 420 TCATGCCCGT CTAATTTTTG TATTCTTAGT AGAGACGGGG TTTCACCATG TTGGCCAGGC 480 TGGTCTCGAA CTCTTGACCT TGTGATCCAC CTGCCTCAGC CTCCCAAAAT GCTGGGATTA 540 CAGGCATGAG CCACCACGCC TGGTCCAGCT TCCATTTTTA ATTAATTAAT TCAATAAACA 600 AGTATGCCCT GGAGTTCACC TGTTATCACG GGGGGTGTAG ACAGAGAGGG AACGCAGACA 660 GGGACAACAC TGGGGGGCTG GGAGGGAAGG AAGAGTCTCC CAACCAAGGC GAGAGGGTTT 720 GCTCTTCTGC CTGGCAGACA CATCTCAGTG AGGCTGGTTC TCTACTTCCA AAACATTCAG 780 AATGACTTTG TTCCTCTCAT GGGAACGGGT GGGGAAGGCA AGGCCTCAAA ACAAAGGCTA 840 ACTTGTGGTA CCAATGGGAG AAGTGGAGAA AGCAAAAAGG CCTAAAAAGG AAGTGGTTCT 900 TGGAAACAGT GTGTCAGCTA CACAGAACAT CTAATTCAGC CACAACCCAG ATCCATGCTG 960 TAGACATGTT CTATATGTTC CCTATACAGA AACGAGAAAA ATCAATTCCT GAGATTTCTT 1020 TTTTTTTTTT TTGAGACGGA GTCTCGCTCT GTCGCCCAGG CTGGAGTGCA GTGGTGCGAT 1080 CTCAGCTCAC TGCAAGCTCC ACCTCCCGGG 1110
|